Kun-Chuan Yang

A novel variant in FOXC1 associated with atypical Axenfeld-Rieger syndrome

Yong Feng, Xue Gao, Yongyi Yuan, 2021, BMC Medical Genomics.

Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site variants in MYO15A

Xue Gao, Guo-jian Wang, Yongyi Yuan, 2022, BMC Medical Genomics.

Genetic Analysis of the LOXHD1 Gene in Chinese Patients With Non-Syndromic Hearing Loss

Xue Gao, Yongyi Yuan, Shasha Huang, 2022, Frontiers in Genetics.

Pathogenic Variants in CEP85L Cause Sporadic and Familial Posterior Predominant Lissencephaly

P. Lockhart, I. Scheffer, H. Mefford, 2020, Neuron.

A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3–4

Xue Gao, Yongyi Yuan, D. Kang, 2022, Molecular genetics & genomic medicine.

Cochlear implantation in a patient with congenital microtia, cochlear hypoplasia, venous anomalies of the temporal bone and laryngomalacia: Challenges and surgical considerations

Yanhui Lu, Xue Gao, P. Dai, 2023, Medicine.

Characterization of SH3GLB1 in the auditory system and its potential role in mitophagy

Yijin Chen, Xue Gao, Guo-jian Wang, 2023, Genes & diseases.